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BruiseMD™ Gel - Indonesia BPOM Medical Device Registration

BruiseMD™ Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603125329. The device is manufactured by NEFTIS LABORATORIES. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REDO MARKETING INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
BruiseMD™ Gel
Analysis ID: AKL 21603125329

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Spain

Authorized Representative

PT. REDO MARKETING INDONESIA

AR Address

Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang

Registration Date

Sep 03, 2021

Expiry Date

Jul 07, 2026

Product Type

Surgical Equipment

Hydrogel wound dressing and burn dressing.

Non Electromedic Non Sterile

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